A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667469



Internal ID9933574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:183360646..183365992hg38UCSC Ensembl
Outerchr3:183360489..183366145hg38UCSC Ensembl
Innerchr3:183078434..183083780hg19UCSC Ensembl
Outerchr3:183078277..183083933hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg385657
hg195657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv899e199
Supporting Variantsessv5404354
SamplesNA18602
Known GenesMCF2L2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667469
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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